Class II — Eos Imaging Inc
| Recalling firm | EOS imaging |
|---|---|
| Registered facility | EOS imaging (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | It was discovered of several generator failures of the EOS System due to failure of its anode controller board that drives the rotation of the X-ray tube anode. |
| Product | EOS X-ray Medical Diagnostic , X-ray Equipment System Digital Radiography used in general radiographic examination. |
| Quantity | 12 EOS Systems installed in the US |
| Distribution | Nationwide distribution |
| Initiated | 2012-06-19 |
| Classified | 2012-09-28 |
| Terminated | 2013-09-16 |
| Recall number | Z-2072-2012 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Eos Imaging Inc (Z-2072-2012).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/62621/
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